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Trifluoroacetic acid → HCID 22080535、化合物

HRID 1047832
ノート
印刷プレビュー

反応式

HRID 1047832 の反応式
[CH2:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1([C:13]([OH:15])=[O:14])[C:10]([OH:12])=[O:11].F[C:17](F)(F)[C:18](O)=O>C(Cl)Cl>[CH2:17]([O:11][C:10]([C:2]1([C:13]([OH:15])=[O:14])[CH2:3][C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[CH2:1]1)=[O:12])[CH3:18]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 6422Trifluoroacetic acidHCID 2519571,3-Dihydroindene-2,2-dicarboxylic acid

生成物 1

HCID 22080535HCID 22080535、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

A 200 mL round bottom flask is charged with indan-2,2-dicarboxylic acid tent-butyl ester ethyl ester (8.69 g, 29.93 mmol). DCM (40 mL) and a stirring bar are added. Stirring is initiated. Trifluoroacetic acid (20.0 mL, 269 mmol) is added. After 20 h, tlc analysis (silica, 1:1 ethyl actetate:heptanes), indicates complete consumption of starting material. The reaction mixture is diluted with DCM (50 mL) and evaporated under reduced pressure. The resultant oil is diluted with DCM (55 mL) and evaporated under reduced pressure. The resultant oil is diluted with toluene (50 mL) and evaporated under reduced pressure by pumping to constant weight to give 6.78 g of white solid material.

後処理

  1. customconsumption of starting material
  2. additionThe reaction mixture is diluted with DCM (50 mL)
  3. customevaporated under reduced pressure
  4. additionThe resultant oil is diluted with DCM (55 mL)
  5. customevaporated under reduced pressure
  6. additionThe resultant oil is diluted with toluene (50 mL)
  7. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-1d3a4debfbdd4671add4c3358639c907
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08569535B2

反応ノート

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